Polymorphisms of pro-inflammatory genes and prostate cancer risk: a pharmacogenomic approach

被引:32
作者
Caruso, Calogero [1 ,2 ]
Balistreri, Carmela Rita [1 ]
Candore, Giuseppina [1 ]
Carruba, Giuseppe [1 ,3 ]
Colonna-Romano, Giuseppina [1 ]
Di Bona, Danilo [1 ,2 ,4 ]
Forte, Giusi Irma [1 ,5 ]
Lio, Domenico [1 ,5 ]
Listi, Florinda [1 ]
Scola, Letizia [1 ,2 ,5 ]
Vasto, Sonya [1 ,2 ]
机构
[1] Univ Palermo, Dipartimento Biopatol & Metodol Biomed, Grp Studio Immunosenescenza, Palermo, Italy
[2] Osped Univ, Palermo, Italy
[3] ARNAS Osped Civ, Dipartimento Oncol, Palermo, Italy
[4] CNR, Ist Biomed & Immunol Mol, Palermo, Italy
[5] Univ Palermo, Dipartimento Biopatol & Metodol Biomed, Cattedra Patol Clin, Palermo, Italy
关键词
Aging; Genetics; Inflammation; Longevity; Pharmacogenomics; Prostate cancer; TOLL-LIKE-RECEPTORS; GROWTH-FACTOR-BETA; PROMOTES TUMOR-GROWTH; NF-KAPPA-B; MYOCARDIAL-INFARCTION; ALZHEIMERS-DISEASE; SEQUENCE VARIANTS; ANDROGEN BIOSYNTHESIS; AROMATASE EXPRESSION; INTERLEUKIN-18; GENE;
D O I
10.1007/s00262-009-0658-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this paper, we consider the role of the genetics of inflammation in the pathophysiology of prostate cancer (PCa). This paper is not an extensive review of the literature, rather it is an expert opinion based on data from authors' laboratories on age-related diseases and inflammation. The aim is the detection of a risk profile that potentially allows both the early identification of individuals at risk for disease and the possible discovery of potential targets for medication. In fact, a major goal of clinical research is to improve early detection of age-related diseases, cancer included, by developing tools to move diagnosis backward in disease temporal course, i.e., before the clinical manifestation of the malady, where treatment might play a decisive role in preventing or significantly retarding the manifestation of the disease. The better understanding of the function and the regulation of inflammatory pathway in PCa may help to know the mechanisms of its formation and progression, as well as to identify new targets for the refinement of new treatment such as the pharmacogenomics approach.
引用
收藏
页码:1919 / 1933
页数:15
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